FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4162504 · Received October 10, 2014

Report

Report Number
1531186-2014-04826
Date Received
October 10, 2014
Report Date
September 23, 2014
Manufacturer
JUMAO HEALTHCARE EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER ALLEGED FRAME WAS BENT CAUSING CROSSBAR TO NOT SIT IN THE SEAT SADDLES PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
644019 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO HEALTHCARE EQUIPMENT TREX20RP

Patients

Seq Age Sex Outcome Treatment
1 Other